Allele Registry

Canonical Allele Identifier: PA2826270372

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019721

RCV000084566

RCV000547582

RCV000826088

RCV002272025

ClinVar Variation:

18094

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191230.1:p.Ala695Thr	CA090906 NM_001204301.2:c.2083G>A